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HS Code |
871230 |
| Chemicalname | 4-Methoxycinnamonitrile |
| Casnumber | 19943-29-2 |
| Molecularformula | C10H9NO |
| Molecularweight | 159.18 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 94-96°C |
| Boilingpoint | 332°C at 760 mmHg |
| Density | 1.13 g/cm3 |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | COC1=CC=C(C=C1)C=CC#N |
As an accredited 4-Methoxycinnamonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Methoxycinnamonitrile is packaged in a 25-gram amber glass bottle with a secure screw cap and safety labeling. |
| Shipping | 4-Methoxycinnamonitrile is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It is typically transported as a solid powder and should be handled in accordance with all local and international regulations for chemical safety. Proper labeling and documentation accompany the shipment to ensure safe and compliant delivery. |
| Storage | 4-Methoxycinnamonitrile should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as oxidizers. Protect the chemical from light and moisture. Label the container clearly, and keep it in a designated chemical storage area, following all relevant safety guidelines and local regulations for hazardous materials. |
Applications of 4-Methoxycinnamonitrile in Industrial Manufacturing4-Methoxycinnamonitrile serves targeted roles in select chemical manufacturing sectors due to its structural features and reactivity. Below, we outline major application fields based on current regulatory, formulation, production, and market practices. 1. Pharmaceutical Intermediates for Anti-inflammatory ActivesThis material functions as a building block in the multi-step synthesis of certain non-steroidal anti-inflammatory drug (NSAID) candidates. Process chemists use its cinnamic core to introduce aryl nitrile functionalities during late-stage modifications, improving target molecule selectivity and pharmacokinetics. Synthesis often involves sequential base-catalyzed reactions followed by selective hydrolysis—controlled under cGMP standards for API-grade intermediates. Industry compliance standards
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2. Fine Fragrance Ingredient ManufacturingSpecialty aroma compound producers utilize this compound as a precursor in the synthesis of methoxy-rich benzylidene notes. It enables access to anisic and balsamic profiles, appearing in high-end fragrance base formulations. The raw material enters controlled condensation or reduction steps, producing signature aldehyde derivatives required for perfume blending lines. Strict IFRA controls apply to ingredient traceability and purity. Industry compliance standards
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3. Agrochemical Intermediate for Fungicide SynthesisResearch-based agrochemical companies incorporate 4-Methoxycinnamonitrile in the construction of heterocyclic scaffolds for triazole-based fungicide development. The compound provides necessary electron-donating groups for selective cyclization reactions. Formulators closely monitor batch integration and traceability, as regulated by global pesticide registration dossiers. Industry compliance standards
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4. Specialty Chemical Synthesis for UV-Absorber ComponentsProducers of advanced UV-absorbing additives in plastics and coatings specify this material for introduction of cinnamic backbone motifs during primary assembly. Its electron-rich character enhances the efficiency of subsequent cycloaddition and etherification steps, ultimately improving UV-B protection in end formulations. Batch-to-batch consistency is validated by spectroscopic and chromatographic controls in line with material standardization protocols. Industry compliance standards
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5. Dye Intermediate in Organic Pigment ManufacturingManufacturers of high-performance organic pigments employ this raw material as a precursor for aryl nitrile-modified anthraquinone or azo dye structures. Its functional group allows introduction of color-shifting and fastness-improving elements during coupling or diazotization steps. Integration protocols demand tracking its use within REACH and TSCA restrictions and ensuring minimal trace impurities for export-grade pigment dispersions. Industry compliance standards
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6. Building Block for Liquid Crystal Monomer SynthesisProducers of specialty monomers rely on 4-Methoxycinnamonitrile for constructing aryl-cinnamyl building blocks in high-performance liquid crystal mixtures. Its nitrile group imparts improved mesogenic order, critical for display panel precursor compounds. The material enters condensation or cross-coupling reactions under monitored conditions, supporting requirements of the electronics and flat panel industry supply chain. Industry compliance standards
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At our factory, the journey with 4-Methoxycinnamonitrile began out of a need for more dependable synthetic intermediates in flavors and pharmaceuticals. As a team with deep roots in aromatic chemistry, we noticed that the nitrile versions of cinnamon derivatives performed with more selectivity and cleaner downstream processing than comparable aldehydes or acids. This insight led us to concentrate R&D efforts on optimizing the synthesis and purification of 4-Methoxycinnamonitrile, which now stands among the more relied-upon intermediates on our production line. Our experience underscores its practical differences from related compounds, both in handling and performance.
Our 4-Methoxycinnamonitrile carries the CAS number 37951-94-7 and its formula, C10H9NO, results in a molecule with unique reactivity in the cinnamic core. Over the years, persistent attention to raw material quality and reaction conditions has allowed us to supply batches exceeding 98% assay by GC, with controlled residual solvents and trace-side products. Particle size remains consistent. Moisture levels, checked batch-to-batch, fall below common impurity thresholds that often trouble downstream usage. Each lot completes in-house NMR, IR, and mass spectrometry verification following synthesis. This standard comes from lived experience. Inconsistent batches can cripple project timelines for our downstream customers, so strict analytics have become non-negotiable.
We run 4-Methoxycinnamonitrile synthesis using controlled condensing of 4-methoxybenzaldehyde with malononitrile, followed by dehydration. Scale-up wasn’t trivial: Reaction temperature shifts, even by a few degrees, swung side-product profiles and kept us vigilant during scale transfer from kilo lab to pilot plant. Regular calibration of glass and stainless reactors kept metal leaching negligible, shielding product from contamination that might impact downstream reactivity in fine chemistry. Sealed handling after work-up ensures light and air don’t trigger unintended polymerization; storage protocols learned the hard way, after early batches exhibited subtle yellowing when left unchecked. Drums are shielded and sealed before shipping, as even a few ppm of external contaminants can affect reproducibility in customer syntheses.
Compared with the widely used 4-methoxycinnamaldehyde or cinnamic acid nitriles, our 4-Methoxycinnamonitrile brings a different set of working properties to the lab bench. Its nitrile group adds electron-withdrawing character, pushing reactivity without raising volatility. Handling it doesn’t fill the work area with overpowering odors, and the relatively high melting point makes for straightforward solid dosing. In multistep synthesis, this small property matters—technicians move with confidence, not rushing to avoid fume build-up. The nitrile function tolerates a wider range of bases and nucleophiles during downstream steps, boosting yields for certain amide and heterocycle targets without nearly as many side products as with aldehydes. We’ve heard repeatedly from partners making agrochemical or fragrance intermediates that this simplifies both reaction monitoring and purification.
Direct experience with clients across the pharmaceutical, flavor, and materials industries guides our understanding of the role this molecule plays. For pharmaceutical chemists, it enters cyclizations and additions—producing scaffolds that might otherwise be tricky or hazardous. With its electron-rich methoxy and the polar nitrile, the aryl–alkene backbone enters Diels-Alder reactions and Michael additions with surprising yields even at medium temperatures. Feedback from a specialty fragrance house pointed toward the signature soft cinnamon-like warmth preserved in final blends. Their technical staff commented that the methoxy modification altered volatility compared to non-methoxylated analogues, providing both depth and persistence in aroma formulations.
Polymer chemists, in search of rigid or cross-linkable structures, appreciate its stability and functional handles. Unlike heavier halo-cinnamonitriles, this methoxy-substituted nitrile doesn’t introduce corrosivity or pose tricky disposal concerns following standard aryl-alkene polymerizations. In our own process development, the compound outperformed several other nitriles in terms of shelf stability and compatibility with common solvents. This originated from our early pilot runs, tuning base and dehydrating agent ratios for cleaner conversion and easier isolation.
Years of direct production have highlighted where our standards make a difference. Many downstream users expressed frustration with discoloration or trace side reactions from poorly made material purchased elsewhere, especially in complex multi-step syntheses. Careful solvent exchanges—developed on the shop floor—help strip out minor colored impurities. We deliberately avoid high-shear grinding or excessive milling to keep particle sizes right-sized for handling but not overly dusty. We test for and document trace solvent remnants by both GC and headspace techniques before any lot goes out the door.
In fluid-bed and continuous flow processes, our product’s tight physical specs cut down equipment fouling and cleaning time, earning comments from technical staff trying to eliminate unplanned downtime. The difference between a highly consistent, clean-synthesized batch and a lesser one appears right away in both analytical data and actual workability, not in marketing speak or spec sheets. Chemists see fewer side reactions, smoother filtration, and less backtracking on purification steps. That came only from batch records and lively discussions with those actually doing the scale-up and pilot work.
The average drum shipped from our plant has been handled more than a dozen times by eyes familiar with the material. We keep packaging tight, avoid heat exposure, and reject any signs of odd coloration at each point in handling. Stackable drums proved best for both safety and product flow, and it took several years to get packaging right, balancing protection with transport efficiency. Our storage technicians carefully log drum positions and rotation schedules in the climate-controlled warehouse. These seemingly simple details can matter more to product shelf-life than the more obvious points on a spec sheet. Our technical support lines up with real production experience, not abstract product codes.
In daily manufacturing practice, we work with a range of aromatic nitriles: unsubstituted cinnamonitrile, halogenated analogues, and varied alkoxy-derivatives. The methoxy group on the para position changes not only electronic character but also processability. 4-Methoxycinnamonitrile consistently provides superior purity and ease of crystallization. By contrast, halo-cinnamonitriles and similar derivatives bring extra regulatory baggage and corrosivity issues that complicate waste handling and plant maintenance.
Over time, comparative runs in our pilot reactors showed that this methoxy variant produces less waste and gives cleaner filter cakes, with a lower risk of plugging lines or crusting on steel. This holds for both gram-scale and ton-scale operations. The learned lesson has been that process hang-ups are often about small physical property differences—just a trace difference in melting or solubility means the difference between a routine filtration and hours at the press. This methoxy nitrile rarely disappoints in that regard.
We have always found the real value of 4-Methoxycinnamonitrile comes out not in published papers, but in the hands-on work with chemists tackling scale-up or custom synthesis projects. Product managers and researchers contact us with details on project bottlenecks—feedback that shapes how we refine purification or logistics. Pharmaceutical and flavor formulators noted that the consistent performance batch-to-batch supports both regulatory filings and internal validation. Reliability of supply and analytical depth, proven in our stability testing protocols, turn what could be a commodity chemical into a reliable building block for innovation.
Our technical staff, many with decades of hands-on fine chemical production under their belts, know the consequences of tiny variances in impurity profile or color. They’ve seen production lines slow or fail when inconsistency creeps in. We share our findings openly with customers, providing direct access to chemists who made and tested their product. This culture emerges from hard experience: There are no shortcuts in aromatic nitrile production. Every lot tells a story, and our records keep those stories consistently positive.
It’s easy to issue a certificate of analysis; delivering a shipment that meets specs under real-world conditions requires more. Our quality system traces every batch back to origin, with archived analytical data and retained samples. Research teams and QA auditors often request detailed histories—often, unexpected questions arise weeks or months after delivery. Our production team can immediately access batch chromatograms or synthesis notes, so customers stay fully informed. We keep lines of communication open and encourage plant visits and audits, recognizing the value of transparency in building trust.
Handling hazardous substances day in and day out, our safety team maintains robust training around every step of the production and filling process. Employees undergo regular safety drills specific to nitrile and aryl-alkene materials, ensuring familiarity with both industrial hygiene and environmental stewardship. We design facility upgrades with responsible waste handling and raw material conservation at the forefront, knowing too well that one mismanaged drum can impact not only a batch’s outcome but also relationships with neighbors and regulators.
We routinely support R&D teams testing novel reactions or scaling up pilot projects. Sharing our internal application notes and process improvements can shave weeks off method development timelines. Recent collaborations included assessment of new cyclization strategies using 4-Methoxycinnamonitrile, and our in-house data helped partners swiftly home in on optimal solvents and catalysts. Timely response to changing requirements and scaling plans creates value for every kilogram shipped. Our staff view each inquiry as an extension of our process, aiming not simply to fulfill orders, but to support breakthroughs in end applications.
In pilot campaigns, unpredictability cut from external suppliers’ unknown impurity profiles stalls progress. Direct collaboration on analytical methods, impurity tracking, and sampling protocols helps avoid these pitfalls. We share detailed impurity maps and robust handling recommendations, learned through repeated, painstaking batch trials. The benefit appears in fewer failed experiments, faster regulatory submissions, and shorter overall project cycles.
Our drive to supply 4-Methoxycinnamonitrile extends into sustainable sourcing and minimized environmental impact. We source key raw materials from suppliers with documented, traceable compliance records and regularly audit upstream practices. In our plant, waste solvent streams are recovered and recycled whenever possible. We minimize off-gas emissions by engineering closed-loop systems and strictly manage process water to avoid discharge issues. Continued investment in environmental controls safeguards not just compliance but reputation—both ours and our customers’. The broader community expects chemical manufacturers not only to meet regulations but also to lead in best practices. A reliable molecule begins with responsible stewardship all the way to the end user.
Our experience with 4-Methoxycinnamonitrile spans from trial-scale synthesis in glassware to multi-ton campaigns in steel reactors. Over the years, incremental process improvements have steadily shaped how the molecule reaches the customer. Early incidents—like color shifts from poorly timed work-ups or unexpected reaction exotherms—taught us to never underestimate the devil in the details. Constant vigilance to process controls and genuinely listening to user feedback have driven us to fine-tune every parameter, from raw material sourcing to final shipping conditions.
Team members spanning R&D, production, and quality control work together, sharing wins and setbacks in open forums. This internal transparency keeps failures from becoming routine and successes from turning into complacency. Every improvement, from solvent recovery upgrades to analytical trickle-down, directly benefits those relying on our 4-Methoxycinnamonitrile to build value in their own labs. We strive not just to make a molecule, but to make it right—guided by the knowledge that in chemistry, the tiniest oversight can topple weeks of effort down the line.
Markets evolve—regulatory constraints grow stricter, formulator expectations rise, and end users face new challenges. Our plant invests in ongoing analytics, advanced process control, and flexible batch scheduling to stay ready for shifting needs. The strength of 4-Methoxycinnamonitrile lies in adapting to these changes without sacrificing quality or safety. Those committed to discovery and manufacturing need confidence in their chosen building blocks. We aim to prove every day that their trust in our product and team is well placed.
Decades of hands-on work with 4-Methoxycinnamonitrile have shaped our manufacturing ethos: Meticulous process management, transparent communication, and continuous technical support define our commitment to partners large and small. Each lot reflects the sum of hundreds of incremental improvements, all rooted in attention to the realities of chemical manufacturing. By standing with our users, we keep learning, adapting, and building supply chains on reliability, safety, and trust. Our 4-Methoxycinnamonitrile stands ready to serve as both the backbone of continued innovation and a testament to the value of true manufacturer experience.